Gene therapy for epilepsy: resculpturing synaptic transmission with neuropeptides
type: CreativeWork
description: Intractable seizures and lack of effective antiepileptic drugs (AED) are severe and common conditions affecting many patients with epilepsy. Thus, there is an urgent need to develop new therapies in epilepsy. The search for novel treatments has identified several neuropeptide systems as potential targets for future therapeutic interventions. The neuropeptide Y (NPY) may represent one such target, as it plays a key role in controlling excitability in the hippocampus by suppressing glutamatergic transmission. If manipulated, the NPY system may be capable of restoring the imbalance between excitation and inhibition occurring in the epileptic brain. Indeed, emerging evidence has established a proof-of-principle for viral vector-mediated transfer of gene and expression of NPY in epileptogenic regions of the brain, providing effective suppression of both acute and chronic seizures in animal models of epilepsy. Therefore, NPY gene therapy strategies are currently under intense investigation and clinical trials are forthcoming. To implement an effective NPY gene therapy in patients, as well as to extend our general knowledge of how transgene NPY may act in the brain, the receptor subtypes mediating the antiepileptic action of NPY needs to be determined. Moreover, the mechanisms underlying the seizure-suppressant effects of transgene NPY are not well understood. Particularly, we need to know under which circumstances transgene NPY is released, and whether and how it acts on synaptic transmission within the area of viral vector transduction. In this thesis, evidences are provided showing that NPY is mediating its antiepileptic effect through activation of both Y2 and Y5 receptors in the hippocampus, and predominately via Y5 receptors in extra-hippocampal areas. Moreover, in rats, hippocampal NPY gene therapy generates long-lasting and neuronal-specific overexpression of transgene NPY. This is not associated with alterations in basal synaptic transmission, probably due to mino…
abstract: Intractable seizures and lack of effective antiepileptic drugs (AED) are severe and common conditions affecting many patients with epilepsy. Thus, there is an urgent need to develop new therapies in epilepsy. The search for novel treatments has identified several neuropeptide systems as potential targets for future therapeutic interventions. The neuropeptide Y (NPY) may represent one such target, as it plays a key role in controlling excitability in the hippocampus by suppressing glutamatergic transmission. If manipulated, the NPY system may be capable of restoring the imbalance between excitation and inhibition occurring in the epileptic brain. Indeed, emerging evidence has established a proof-of-principle for viral vector-mediated transfer of gene and expression of NPY in epileptogenic regions of the brain, providing effective suppression of both acute and chronic seizures in animal models of epilepsy. Therefore, NPY gene therapy strategies are currently under intense investigation and clinical trials are forthcoming. To implement an effective NPY gene therapy in patients, as well as to extend our general knowledge of how transgene NPY may act in the brain, the receptor subtypes mediating the antiepileptic action of NPY needs to be determined. Moreover, the mechanisms underlying the seizure-suppressant effects of transgene NPY are not well understood. Particularly, we need to know under which circumstances transgene NPY is released, and whether and how it acts on synaptic transmission within the area of viral vector transduction. In this thesis, evidences are provided showing that NPY is mediating its antiepileptic effect through activation of both Y2 and Y5 receptors in the hippocampus, and predominately via Y5 receptors in extra-hippocampal areas. Moreover, in rats, hippocampal NPY gene therapy generates long-lasting and neuronal-specific overexpression of transgene NPY. This is not associated with alterations in basal synaptic transmission, probably due to mino…
author: Toft Sörensen, Andreas
language: eng
keywords: Other Clinical Medicine, LTP, synaptic plasticity, synaptic transmission, electrophysiology, Y5 receptor, Y2 receptor, neuropeptide Y (NPY), hippocampus, gene therapy, epilepsy, memory, activity-dependent release, volume transmission
date published: 2008
date modified: 2026-07-24T03:00:02Z
provider: University of Lund
publisher: Networked Digital Library of Theses and Dissertations
type: WebPage
source organization: Institutionen för kliniska vetenskaper, Lunds universitet